| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152645185-152645438 | Rare:47 | ||||
| chr2:152670262-152670465 | Rare:44 | ||||
| chr2:156334478-156334790 | Rare:68 | ||||
| chr2:156341635-156341825 | Rare:58 | ||||
| chr2:158969666-158969857 | Rare:42 | ||||
| chr2:159728771-159729051 | Common:3; Rare:62 | ||||
| chr2:159753229-159753459 | Common:1; Rare:49 | ||||
| chr2:159764435-159764671 | Rare:56 | ||||
| chr2:159774911-159775092 | Common:1; Rare:33 | ||||
| chr2:159780910-159781078 | Common:1; Rare:51 | ||||
| chr2:159783363-159783755 | Common:3; Rare:98 | ||||
| chr2:160142003-160142120 | Rare:30 | ||||
| chr2:160270288-160270596 | Common:2; Rare:75 | ||||
| chr2:161244613-161244841 | Common:1; Rare:63 | ||||
| chr2:162317912-162318058 | Rare:55; Clinvar:1; Clinvar (benign):1 |